Litcius/Paper detail

Isolable Geminal Bisgermenolates: A New Synthon in Organometallic Chemistry

Manfred Drusgala, Philipp Frühwirt, Gabriel Glotz, Katharina Hogrefe, Ana Torvisco, Roland C. Fischer, Martin Wilkening, Anne‐Marie Kelterer, Georg Gescheidt, Michael Haas

2021Angewandte Chemie International Edition15 citationsDOIOpen Access PDF

Abstract

(R=2,4,6-trimethylphenyl (2 a,b), L=THF for (2 a) or [18]-crown-6 for (2 b)), a new synthon for the synthesis of organometallic reagents. The formation of these derivatives was confirmed by NMR spectroscopy and X-ray crystallographic analysis. The UV/Vis spectra of these anions show three distinct bands, which were assigned by DFT calculations. The efficiency of 2 a,b to serve as new building block in macromolecular chemistry is demonstrated by the reactions with two different types of electrophiles (acid chlorides and alkyl halides). In all cases the salt metathesis reaction gave rise to novel Ge-based photoinitiators in good yields.

Topics & Concepts

SynthonGeminalChemistryElectrophileMetathesisReagentNuclear magnetic resonance spectroscopyOrganometallic chemistryHalideNMR spectra databaseAlkylMedicinal chemistryPolymer chemistryStereochemistryOrganic chemistrySpectral lineCatalysisPolymerizationAstronomyPolymerPhysicsFluorine in Organic ChemistrySynthesis and characterization of novel inorganic/organometallic compoundsRadical Photochemical Reactions